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A convenient synthesis of benzo[g]pyrrolo[3,2-c]quinoline-6,11-diones

Authordc.contributor.authorTapia, Ricardo A. 
Authordc.contributor.authorLópez, Claudio 
Authordc.contributor.authorMorello, Antonio 
Authordc.contributor.authorMaya Arango, Juan 
Authordc.contributor.authorValderrama, Jaime A. 
Admission datedc.date.accessioned2018-12-20T15:20:42Z
Available datedc.date.available2018-12-20T15:20:42Z
Publication datedc.date.issued2005
Identifierdc.identifier.issn00397881
Identifierdc.identifier.other10.1055/s-2005-861802
Identifierdc.identifier.urihttp://repositorio.uchile.cl/handle/2250/158875
Abstractdc.description.abstractThe synthesis of a new class of angular tetracyclic quinones is described. Our strategy involves Diels-Alder reaction of pyrroloquinolinequinone 9, generated in situ from pyrroloquinoline 8, and dienes. The required pyrroloquinoline 8 was prepared in four steps from commercially available compounds. All compounds were tested for trypanocidal activity in vitro against Trypanosoma cruzi epimastigotes. © Georg Thieme Verlag Stuttgart.
Lenguagedc.language.isoen
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceSynthesis
Keywordsdc.subjectBenzo[g]pyrrolo[3,2-c]quinoline
Keywordsdc.subjectDiels-Alder reaction
Keywordsdc.subjectHeterocycles
Keywordsdc.subjectHeterocyclic quinones
Keywordsdc.subjectPyrroloquinoline
Títulodc.titleA convenient synthesis of benzo[g]pyrrolo[3,2-c]quinoline-6,11-diones
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile